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Il Nuovo cimento della Società italiana di fisica. B/Il Nuovo cimento B

Antibunching in absorptive optical bistability

Federico Casagrande, L. A. Lugiato

Published Feb 1, 1980• 40 citations
Publisher
DOI
10.1007/bf02739152

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Phase instabilities in absorptive optical bistability

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Optics Communications•Sep 1, 1989•5 citations
Photon antibunching has been predicted at weak intensities along the lower branch in optical bistability. Existing theories assume large atomic numbers to justify their linearized analysis. From such a theory photon antibunching in absorptive bistability is given for weak intensities by where C is the bistability parameter, μ is the ratio of atomic and cavity decay times, and N is the number of atoms. Clearly this result becomes invalid as the system size is reduced to the limit of a single atom; then g(2) (0) is negative for moderate values of C. I calculate g(2) (0) for the transmitted light from an optical cavity containing a single atom, where the injected field, the atom, and the cavity are all resonant.
We specialize the quantum-statistical theory of optical bistability developed in "Optical Bistability. II" to a low-QQQ cavity. From a linearized Fokker-Planck equation derived in the positive PPP representation, the steady-state correlation matrix and spectrum of fluctuations are calculated. Expressions which normally assume a positive-definite diffusion matrix are shown to be valid for nonpositive-definite diffusion. For absorptive bistability we find agreement with results derived previously by quite different methods. More generally we extend previously published results by including atomic and cavity detunings. We compare the transmitted spectrum for dispersive bistability with that for absorptive bistability, and photon antibunching in dispersive bistability is discussed.
Based on the established theory of photoinduced exciton bleaching of the polymers with nondegenerated ground state,we calculated the transient mirrorless optical bistability of photoexcitation and relaxation processes in the polymers.The results show that the transient saturation absorption mirrorless optical bistabilities and the increasing absorption mirrorless optical bistabilities can be obtained from the ultrafast excitation and relaxation processes in the polymers with nondegenerate ground state,and the switching time of the optical bistabilities is of the order of fs or ps.With the increase of the delay time of the probe pulse relative to pump pulse,the nature of mirrorless optical bistability can change from the saturation absorption optical bistability to increasing absorption optical bistability,and the rate of change is proportional to the speed of relaxation of the photoinduced exciton.